Liquiritin

CAS No. 551-15-5

Liquiritin( Liquiritoside | Likviritin | Liquiritin )

Catalog No. M18791 CAS No. 551-15-5

Liquiritin is sompound extracted from Radix liquiritiae.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 41 In Stock
5MG 37 In Stock
10MG 61 In Stock
25MG 122 In Stock
50MG 184 In Stock
100MG 305 In Stock
200MG Get Quote In Stock
500MG 733 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Liquiritin
  • Note
    Research use only, not for human use.
  • Brief Description
    Liquiritin is sompound extracted from Radix liquiritiae.
  • Description
    Liquiritoside is a flavonoid complex isoalted from Glycyrrhizae radix.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Liquiritoside | Likviritin | Liquiritin
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Phospholipase
  • Recptor
    Others
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    551-15-5
  • Formula Weight
    418.39
  • Molecular Formula
    C21H22O9
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 150 mg/mL 358.52 mM
  • SMILES
    C1[C@H](Oc2c(C1=O)ccc(c2)O)c1ccc(cc1)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
  • Chemical Name
    (S)-7-hydroxy-2-(4-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Zhang W, et al. Biomed Chromatogr. 2014 Sep;28(9):1271-7.
molnova catalog
related products
  • PHPS1

    PHPS1 is an inhibitor of Shp2. PHPS1 efficiently inhibits activation of Erk1/2 by the leukemia-associated Shp2 mutant, Shp2-E76K, and blocks the anchorage-independent growth of a variety of human tumor cell lines.

  • Darapladib

    A potent Lp-PLA2 inhibitor with IC50 of 0.25 nM.

  • PACOCF3

    PACOCF3 (Palmityltrifluoromethylketone) (Palmityltrifluoromet hylketone) is an inhibitor of Ca(2+)-independent phospholipase A2(PLA2) with an IC 50 of 3.8 μM.